2.1.1 Cell Structure Flashcards

(48 cards)

1
Q

State differences between eukaryotic and prokaryotic cells

A
  • Prokaryotes don’t have a nucleus, eukaryotes do
  • Prokaryotes are bacteria, eukaryotes are animal and plant cells
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2
Q

Describe a virus

A
  • non-cellular
  • contains no cytoplasm or organelles
  • no chromosome, just DNA and RNA strands
  • enclosed in a protein coat
  • depends on cells for metabolism and reproduction
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3
Q

Name organelles of an animal cell

A
  • mitochondria
  • plasma membrane
  • centrioles
  • Golgi apparatus
  • nucleus
  • lysosome
  • rough er
  • smooth er
  • ribosome
  • cell surface membrane
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4
Q

Describe the structure and function of a nucleus

A

Structure
Nuclear envelope:
- outer membrane
- inner membrane
- pores in nuclear envelope

  • nucleoplasm (made from chromatin)
  • nucleolus (dark region of chromatin)
  • largest organelle

Function
- stores genetic information in DNA
- DNA replication occurs in the nucleus

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5
Q

Describe the structure and function of a ribosome

A

Structure
- very small
- mostly found on ER (makes it rough)
- made of RNA
- no membrane
- made from two subunits
- 70s (smaller) in prokaryotic cells
- 80s in eukaryotic cells

Function
- carries out protein synthesis

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6
Q

Describe the structure and function of the rough endoplasmic reticulum

A

Structure
- covered in ribosomes
- forms cisternae (flattened sacs)
- membrane made from phospholipid bilayer
- membranes are continuous with nuclear envelope

Function
- transports protein around the cell and the Golgi body
- holds ribosomes responsible for protein synthesis

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7
Q

Describe the structure and function of the smooth endoplasmic reticulum

A

Structure
- forms cisternae (flattened sacs)
- membrane made from phospholipid bilayer

function
- site of production and transport of lipids/steroids

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8
Q

Describe the structure and function of the Golgi body/apparatus

A

Structure
- flatterned membrane-bound sacs

Function
- receives proteins from ribosomes
- proteins and lipids then become modified to produce glycoproteins and glycolipids (carbohydrate is added) then packaged into vesicles
- vesicles transport glycoproteins and glycolipids to the cell membrane, to be secreted by exocytosis
- also produces lysosomes, which contain lytic enzymes which breakdown bacteria and worn out organelles

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9
Q

Describe the structure and function of the mitochondria

A

Structure
- outer + inner membrane
- matrix, where DNA is found (space inside)
- inner membrane is folded to form cristae
- sausage shaped

function
- site of aerobic respiration
- ATP is formed here
- have circular DNA and 70s ribosomes (suggest they could have evolved from bacteria)

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10
Q

Describe the structure and function of the cytoskeleton

A

Structure
- microfilaments of actin
- microtubules made of tublin

Function
- micro filaments move against each other allowing cellular movement
- provides strength
- stabilises, supports, strengthens the cell
- holds organelles in place
- transport within the cell
- make up the spindle fibres and centrioles used in cell devision
- used to move flagella and cilia

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11
Q

Describe and explain vesicle and lysosome transport

A
  • cytoskeleton (microtubules) provide a pathway
  • 2 motor types- dynein + kinesin, which use ATP
  • microtubules can be extended and broken down
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12
Q

Suggest processes that rely on the cytoskeleton for movement

A
  • movement of chromosomes in cell division
  • movement of cytoplasm in cytokinesis
  • movement of organelles
  • movement of RNA in protein synthesis
  • movement of proteins
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13
Q

Describe the structure and function of centrioles

A

Structure
- small tubes of protein fibres
- found near the nucleus in animal cells
- not found in plant cells

Function
- form spindle fibres for cell division
- move chromosomes during nuclear division

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14
Q

Describe the structure and function of flagella and cilia

A

Structure
- nine microtubules arranged in a circle with two at the centre

Function
- movement caused by ATP
- required mitochondria and cytoskeleton to function
- used by sperm cells and ciliated epithelial cells

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15
Q

Describe the structure and function of micro villi

A

Structure
- folds in the plasma membrane of animals cells

Function
- increases surface area for a faster rate of diffusion

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16
Q

Name the organelles of a plant cell

A
  • cell wall
  • cell surface membrane
  • large permanent vacuole
  • nucleus
  • chloroplasts
  • mitochondria
  • cytoplasm
  • lysosome
  • rough er
  • smooth er
  • ribosomes
  • Golgi body
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17
Q

Describe and explain the components of a chloroplast

A
  • outer and inner membrane
  • oil droplets contacting lipids used for making/ repairing membranes (as they are made from phospholipids)
  • grana made from stacks of disks called thylakoids
  • thylakoids contain the pigment chlorophyll
  • intergranal lamellae are membranes that link the grana together
  • the Stroma is fill with fluid + starch grains
  • contains 70s ribosomes and circular DNA (suggests they evolved from bacteria)
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18
Q

Name 3 important adaptations of chloroplasts

A
  • grana have a large surface area for attachment of lots of chlorophyll molecules
  • chloroplasts have DNA and ribosomes to quickly create protein when needed
  • chloroplasts have oil droplets for making more phospholioid membranes
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19
Q

Describe the structure and function of the cell wall in plant cells

A
  • made from cellulose (a polysaccharide) which is permeable
  • provides strength to the cell, as it has a high tensile strength to stop the cell bursting when water enters
  • makes the cell rigid, which prevents wilting
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20
Q

Describe the structure and function of the cell vacuole

A

Structure
- Membrane bound (tonoplast)
- contains cell sap (weak solution of sugar + salts)

Function
- helps maintain pressure inside cell and keep it rigid
- stop the plant wilting
- can isolate unwanted chemicals

21
Q

Name the parts of the cell protein manufacture requires

A
  • DNA and RNA molecules
  • rough endoplasmic reticulum
  • ribosomes
  • vesicles
  • Golgi body
22
Q

Explain the production of extracellular proteins

A
  1. Genes in nucleus are copied into mRNA (transcription)
  2. mRNA joins with rough ER and ribosome for translation/protein synthesis
  3. A protein is built in the ribosome
  4. Protein is put into a transport vesicle to be transported to the Golgi body
  5. Golgi body process, modifies and packages protein (e.g. makes a glycoprotein)
  6. Golgi body packages protein into a secretory vesicle which moves and fuses to the cell membrane, then released by exocytosis (using ATP)
  7. Golgi body also makes lysosomes which digest worn out organelles
23
Q

Give examples of extracellular proteins which are excreted (4)

A
  • enzymes - amylase/lipase/protease
  • protein hormones - insulin/ADH
  • glycoproteins for cell membrane
  • antibodies
24
Q

Describe the structure of DNA in eukaryotic and prokaryotic cells

A
  • eukaryotic DNA is linear as chromosomes
  • eukaryotic DNA has proteins called histones which organise it into chromosomes
  • prokaryotic DNA is circular
  • prokaryotic DNA has no histones so does not form chromosomes
25
List similarities of eukaryotic and prokaryotic cells
- plasma membrane which controls substances entering and exiting the cell - cytoplasm where most of the metabolic reactions occur - ribosomes for protein synthesis - DNA containing coded information for protein production
26
List differences of prokaryotic and eukaryotic cells
- Eukaryotic: larger cells (20-100um) - Prokaryotic: extremely small (less than 0.5 - 5um) - Eukaryotic: has membrane bound organelles - Prokaryotic: no membrane bound orangelles - Eukaryotic: nucleus containing DNA - Prokaryotic: no nucleus- DNA free in cytoplasm - Eukaryotic: DNA is linear as chromosomes - wound around histone proteins - Prokaryotic: DNA is circular and not wound around histone proteins - Eukaryotic: small 70s ribosomes (18nm) - Prokaryotic: large 80s ribosomes (22nm) - Eukaryotic: cellulose cell wall in plant cells, chitin fungal cell wall, no cell wall in animal cells - Prokaryotic: peptidiglycan cell wall
27
Explain the makeup of cells, tissues, organs and systems
- cells make up all living things - a tissue is a collection of similar cells that are specialised to work together to a particular function - an organ is a collection of different tissues working together to perform a common function - a system is a group of organs working together to perform a particular function
28
What are the two lenses found in a compound light microscope, and how do they work?
1. Objective lens - placed near the specimen 2. Eyepiece (ocular) lens - lens through which the specimen is viewed Objective lens produces a magnified image, which is magnified again by the eyepiece lens
29
What are dry and wet mounts?
1. Dry mount - solid specimen either cut thin or whole with a cover slip on top 2. Wet mount - specimens suspended in water or oil (with refractive index same as glass), cover slip placed at angle to prevent bubbles
30
What are squash and smear slides?
1. Squash slide - wet mount but using a lens tissue apply pressure to the cover slip to squash specimen 2. Smear slide - edge of slide used to smear a specimen then a cover slip is added
31
List important things to do when preparing an onion cell slide
- use forcepts to obtain thin layer + place on slide - use pipette to place 2 stopds on stain on edge of sample - lower cover slip at angle using a mounted needle - use blotting paper to remove excess stain
32
What rules must be followed when drawing a scientific drawing?
- use a piece of plain paper - use a sharp pencil - use at leasat 50% of space - use correct proportions - continous lines - NO shading - use ruled label lines - labels outside diagram - lables don't cross - include a title + magnification
33
Why is staining used on samples?
- makes cells/organelles visible by increasing contrast - allows recognition of different cell types + different organelles
34
What is the difference between gram negative and gram positive bacteria?
Gram negative: Not killed by penicillin as the less vital peptidoglycan cell wall is thinner and covered by a lipopolysaccharide layer Gram positive: Killed by penicillin as it works by reaking down the vital peptidoglycan cell wall
35
When is a differential stain - gram stain used?
To determine whether bacteria are gram negative or gram positive
36
What is the procedure of gram staining?
1. Crystal violet stain applied 2. Alcohol decolorization - alcohol is used to wash away the stain from gram negative cells, leaving them colorless. Gram-positive cells retain the stain due to their thicker peptidoglycan layer. 3. Counterstaining - counterstain is applied to the smear, staining the decolorized Gram-negative cells pink while maintaining the purple color of the gram positive cells 4. Observation - the slide is observed under a microscope to determine the gram reaction of the bacteria
37
What colour does each bacteria stain and why?
Gram positive: Purple, as the alcohol doesn't remove crystal violet because of the thick peptidoglycan wall Gram negative: Pink, as the alcohol washes out the crystal violet due to the thin peptidoglycan cell wall covered by the lipopolysaccharide cell wall - pink counter-stain bindso the cell wall
38
What is leishman's stain used for?
- provides contrast between the cytoplasm and the nucleus - allows the shape of the nucleus to be seen - allows different white blood cells with different shaped nuclei to be seen - red blooc cells not affected as have no nucleus for stain to bind to
39
Define fixing, sectioning, staining and mounting
Fixing: Chemicals like formaldehyde are used to preserve specimens in as near-natural state as possible Sectioning: Specimens are dehydrated with alcohols and then placed in a mould with wax/resin to form a hard block - thinly sliced with a knife Staining: Specimens treated with multiple coloured chemicals to show different strutures Mounting: Specimens secured to microscope slide and cover slide placed on top
40
What are the advantages and disadvantages of using a light microscope?
**Advantages** - portable - takes up little space - specimens easy to prepare - can see cells and often nucleus - colour visible **Disadvantages** - low resolution (200nm) as wavelength of light too long - cannot see small organelles or details of organelles
41
Define magnification and resolution
Magnification: The degree to which the size of an image is larger than the object itself Resolution: The ability to see two objects tha are close together as separate objects and see in detail
42
How do electron microscopes work and why do they have a higher resolution compared to a light microscopes?
- beam of electrons focused by electromagnets through or onto the surface of a specimen - electron microscopes use electrons to take images, which have a much short wavelength (0.2nm), so have a higher resolution
43
What are the two types of electron microscope, how do they work, and what type of image do they produce
**Transmission electron microscope (TEM)** - a beam of electrons is transmitted through a specimen and focused to produce a 2D image - used to view the ultra structure of cells and organelles **Scanning electron microscope (SEM)** - a beam of electrons is sent across a specimen and reflected electrons are collected to produce a 3D image - used to view the 3D shape of the surface of cels and organelles and their surface features
44
What is the magnification and resolution of each type of electron microscope and a light microscope?
**Transmission electron microscope (TEM)** Magnification: x500,000 Resolution: 0.05 - 2nm **Scanning electron microscope (TEM)** Magnification: x100,000 Resolution: 5 - 50nm **Light microscope** Magnification: x1500 Resolution: 200nm
45
What are the advantages and disadvantages of using an electron microscope?
**Advantages** - higher resolution - higher magnification - shorter wavelength - can see ultra structure **Disadvantages** - cannot view living cells - must be in vacuum - no colour images - specimen must be thin - artefacts may appear (structures produced during preparation process) - have to be treated with metal (lead) salts
46
List units used when measuring smaller specimens, their units and how to convert between them
- milimetre (mm) - 1000μm - micrometre (μm) - 1000nm - nanometre (nm)
47
How is magnification calculated?
Magnification = Image size / real object size
48
What is an eyepiece graticule and stage micrometer?
Eyepiece graticule: Placed into the eyepiece lens - used to measure specimens seen udner the microscope. Will not change size when magnification is changed. Needs to be calibrated Stage micrometer: Goes on the stage of the microscope - a microscope slide with a scale etched into it. Is a known size (e.g. 1mm). Used to calibrate eyepiece graticle